Researchers
Kostić, Vladimir
Results 101-120 of 555
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | Evaluation of blood lymphocyte subsets and monocyte function in Alzheimers disease![]() | Isaković, Anđelka M. | Conference Paper | Mp. category will be shown later |
| 2019 | Results of clinical exome analysis in rare neurodegenerative disorders in Serbian population![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Tracking cortical changes throughout cognitive decline in Parkinson's disease: a longitudinal MRI study![]() | Canu, Elisa; Agosta, Federica; Stojković, Tanja | Conference Paper | Mp. category will be shown later |
| 2019 | KRIT1 Gene Analysis In Serbian Patients With Familial Cerebral Cavernous Malformation![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Applications of the European Parkinsons Disease Association sponsored Parkinsons Disease Composite Scale (PDCS) | Balestrino Roberta; Alberto Hurtado-Gonzalez Carlos; Stocchi Fabrizio; Radicati Fabiana Giada; Chaudhuri K. Ray; Rodriguez-Blazquez Carmen; Martinez-Martin Pablo; Adarmes Astrid D.; Mendez-del-Barrio Carlota; Ariadne Vakirli;
Aschermann Zsuzsanna; Juhasz Annamaria; Harmat Mark; Bostantjopoulou Sevasti; Corbo Massimo; Grassi Andrea; Dellaporta Dionysia; Falup-Pecurariu Cristian; Diaconu Stefania; Giagkou Nikolaos; Guekht Alla; Popov Georgy; Gurevich Tanya; Johansson Anders; Sundgren Mathias; Kefalopoulou Zinovia; Ellul John; Kostić, Vladimir S.
| Article | 21aM21a |
| 2019 | Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: First experience![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Artificial intelligence for assisting diagnostics and assessment of Parkinson's disease-A review![]() | Belić, Minja; Bobić, Vladislava | Reviews | 22M22 |
| 2019 | Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | NOTCH3 mutations in Serbian CADASIL patients![]() | Janković, Milena Z. | Conference Paper | Mp. category will be shown later |
| 2019 | Longitudinal cortical changes associated with apathy in Parkinson's disease![]() | Agosta, Federica; Imperiale, Francesca; Canu, Elisa; Stojković, Tanja | Conference Paper | Mp. category will be shown later |
| 2019 | Impaired intracortical inhibition predicts response to medication in Parkinson's disease patients![]() | Filipović, Saša R. | Conference Paper | Mp. category will be shown later |
| 2019 | The frequency of C9orf72 repeat expansion beyond ALS/FTD spectrum in Serbian patients with neurodegenerative disorders![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | An Expert System for Quantification of Bradykinesia Based on Wearable Inertial Sensors![]() | Bobić, Vladislava | Article | 21M21 |
| 2019 | Extensive validation study of the Parkinson's Disease Composite Scale | Martinez‐Martin, P.; Radicati, F. G.; Rodriguez, Blazquez C.; Wetmore, J.; Kovacs, N.; Ray, Chaudhuri K.; Stocchi, F.; Vuletic, Vladimira; Falup‐Pecurariu, Cristian; Diaconu, Ştefania;
Johansson, Anders; Sundgren, Mathias; Simitsi, Athima; Stefanis, Leonidas; Gurevich, Tanya; Migirov‐Sanderovich, Angel; Ezra, Adi; Guekht, Alla; Popov, Georgy; Stamelou, Maria; Giagkou, Nikolaos; Stefani, A.; Cerroni, R.; Corbo, Massimo; Grassi, Andrea; Dellaporta, Dionysia; Tsolaki, Magda; Ariadne, Vakirli; Kefalopoulou, Zinovia; Ellul, John; Mir, Pablo; Adarmes, Astrid D.; Méndez‐del‐Barrio, Carlota; Skorvanek, Matej; Necpal, Jan; Bostantjopoulou, Sevasti; Zoe, Katsarou; Minar, Michal; Simu, Mihaela; Rosca, Cecilia; Popovici, Maria; Kostić, Vladimir
| Article | 21M21 |
| 2019 | Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy![]() | Dawod, Phepy G. A.; Rovčanin, Branislav R. | Conference Paper | Mp. category will be shown later |
| 2019 | Correlation of selected polymorphisms in COMT, DAT (SL6A3), DRD2, and ANKK1 genes and complications of long-term levodopa treatment in patients with idiopathic Parkinsons disease![]() | Radojević, Branislava | Conference Paper | Mp. category will be shown later |
| 2019 | Functional network connectivity predicts spreading of cortical atrophy in Parkinson's disease![]() | Agosta, Federica; Basaia, Silvia; Zahedmanesh, Homa; Stojković, Tanja | Conference Paper | Mp. category will be shown later |
| 2019 | Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients![]() | Mitropoulos, Konstantinos; ...; Dobričić, Valerija S. | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy![]() | Dawod, Phepy G. A.; Rovčanin, Branislav R.; Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia![]() | Perić, Stojan Z. | Conference Paper | Mp. category will be shown later |
